Clin2
NCT07169565Possibly a fitNot yet recruiting

Adding bendamustine and rituximab for stable Waldenström macroglobulinemia

Waldenström Macroglobulinemia (WM)

Treatments studied

Part of Blood & lymphatic, Cancer, Heart & circulation, Immune system & allergy clinical trials.

This study tests a new approach for people with Waldenström macroglobulinemia who have already been on ibrutinib and are doing well but not completely better. It adds two more medicines (bendamustine and rituximab) to see if this combination can achieve a deeper response and allow you to stop treatment after a set period.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1
Enrollment
21 people
Ages
18 years to 75 years
Study type
Interventional

Who can take part

  • You are between 18 and 75 years old and have been diagnosed with Waldenström macroglobulinemia that has a specific gene change called MYD88 L265P.
  • You have been taking ibrutinib for at least 12 rounds, your disease has gotten better but not completely gone, and you are currently stable on this medicine.
  • You have not had serious side effects from ibrutinib that required stopping it (no grade 3 or higher side effects).
  • You have never been treated with the combination of bendamustine and rituximab (BR).
  • Your blood counts and liver and kidney function must be within certain limits (your doctor will check this with blood tests).
  • You have not had another cancer (except some skin cancers or early-stage cancers) in the past year, and you do not have serious heart, bleeding, or other medical conditions.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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